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Shape-Dependent Optoelectronic Cell Lysis**

We show an electrical method to break open living cells amongst a population of different cell types, where cell selection is based upon their shape. We implement the technique on an optoelectronic platform, where light, focused onto a semiconductor surface from a video projector creates a reconfigu...

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Detalles Bibliográficos
Autores principales: Kremer, Clemens, Witte, Christian, Neale, Steven L, Reboud, Julien, Barrett, Michael P, Cooper, Jonathan M
Formato: Online Artículo Texto
Lenguaje:English
Publicado: WILEY-VCH Verlag 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4441254/
https://www.ncbi.nlm.nih.gov/pubmed/24402800
http://dx.doi.org/10.1002/anie.201307751
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author Kremer, Clemens
Witte, Christian
Neale, Steven L
Reboud, Julien
Barrett, Michael P
Cooper, Jonathan M
author_facet Kremer, Clemens
Witte, Christian
Neale, Steven L
Reboud, Julien
Barrett, Michael P
Cooper, Jonathan M
author_sort Kremer, Clemens
collection PubMed
description We show an electrical method to break open living cells amongst a population of different cell types, where cell selection is based upon their shape. We implement the technique on an optoelectronic platform, where light, focused onto a semiconductor surface from a video projector creates a reconfigurable pattern of electrodes. One can choose the area of cells to be lysed in real-time, from single cells to large areas, simply by redrawing the projected pattern. We show that the method, based on the “electrical shadow” that the cell casts, allows the detection of rare cell types in blood (including sleeping sickness parasites), and has the potential to enable single cell studies for advanced molecular diagnostics, as well as wider applications in analytical chemistry.
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spelling pubmed-44412542015-05-26 Shape-Dependent Optoelectronic Cell Lysis** Kremer, Clemens Witte, Christian Neale, Steven L Reboud, Julien Barrett, Michael P Cooper, Jonathan M Angew Chem Int Ed Engl Communications We show an electrical method to break open living cells amongst a population of different cell types, where cell selection is based upon their shape. We implement the technique on an optoelectronic platform, where light, focused onto a semiconductor surface from a video projector creates a reconfigurable pattern of electrodes. One can choose the area of cells to be lysed in real-time, from single cells to large areas, simply by redrawing the projected pattern. We show that the method, based on the “electrical shadow” that the cell casts, allows the detection of rare cell types in blood (including sleeping sickness parasites), and has the potential to enable single cell studies for advanced molecular diagnostics, as well as wider applications in analytical chemistry. WILEY-VCH Verlag 2014-01-13 2014-01-08 /pmc/articles/PMC4441254/ /pubmed/24402800 http://dx.doi.org/10.1002/anie.201307751 Text en © 2014 The Authors. Published by Wiley-VCH Verlag GmbH & Co. KGaA. This is an open access article under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. https://creativecommons.org/licenses/by/4.0/ © 2014 The Authors. Published by Wiley-VCH Verlag GmbH & Co. KGaA. This is an open access article under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Communications
Kremer, Clemens
Witte, Christian
Neale, Steven L
Reboud, Julien
Barrett, Michael P
Cooper, Jonathan M
Shape-Dependent Optoelectronic Cell Lysis**
title Shape-Dependent Optoelectronic Cell Lysis**
title_full Shape-Dependent Optoelectronic Cell Lysis**
title_fullStr Shape-Dependent Optoelectronic Cell Lysis**
title_full_unstemmed Shape-Dependent Optoelectronic Cell Lysis**
title_short Shape-Dependent Optoelectronic Cell Lysis**
title_sort shape-dependent optoelectronic cell lysis**
topic Communications
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4441254/
https://www.ncbi.nlm.nih.gov/pubmed/24402800
http://dx.doi.org/10.1002/anie.201307751
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